TY - JOUR
T1 - Cellular community detection for tissue phenotyping in colorectal cancer histology images
AU - Javed, Sajid
AU - Mahmood, Arif
AU - Fraz, Muhammad Moazam
AU - Koohbanani, Navid Alemi
AU - Benes, Ksenija
AU - Tsang, Yee Wah
AU - Hewitt, Katherine
AU - Epstein, David
AU - Snead, David
AU - Rajpoot, Nasir
N1 - Funding Information:
This work was supported by the UK Medical Research Council (No. MR/P015476/1). NR is also supported by the PathLAKE digital pathology consortium, which is funded from the Data to Early Diagnosis and Precision Medicine strand of the government\220s Industrial Strategy Challenge Fund, managed and delivered by UK Research and Innovation (UKRI).
Funding Information:
This work was supported by the UK Medical Research Council (No. MR/P015476/1). NR is also supported by the PathLAKE digital pathology consortium, which is funded from the Data to Early Diagnosis and Precision Medicine strand of the government\220s Industrial Strategy Challenge Fund, managed and delivered by UK Research and Innovation (UKRI).
Publisher Copyright:
© 2020
PY - 2020/7
Y1 - 2020/7
N2 - Classification of various types of tissue in cancer histology images based on the cellular compositions is an important step towards the development of computational pathology tools for systematic digital profiling of the spatial tumor microenvironment. Most existing methods for tissue phenotyping are limited to the classification of tumor and stroma and require large amount of annotated histology images which are often not available. In the current work, we pose the problem of identifying distinct tissue phenotypes as finding communities in cellular graphs or networks. First, we train a deep neural network for cell detection and classification into five distinct cellular components. Considering the detected nuclei as nodes, potential cell-cell connections are assigned using Delaunay triangulation resulting in a cell-level graph. Based on this cell graph, a feature vector capturing potential cell-cell connection of different types of cells is computed. These feature vectors are used to construct a patch-level graph based on chi-square distance. We map patch-level nodes to the geometric space by representing each node as a vector of geodesic distances from other nodes in the network and iteratively drifting the patch nodes in the direction of positive density gradients towards maximum density regions. The proposed algorithm is evaluated on a publicly available dataset and another new large-scale dataset consisting of 280K patches of seven tissue phenotypes. The estimated communities have significant biological meanings as verified by the expert pathologists. A comparison with current state-of-the-art methods reveals significant performance improvement in tissue phenotyping.
AB - Classification of various types of tissue in cancer histology images based on the cellular compositions is an important step towards the development of computational pathology tools for systematic digital profiling of the spatial tumor microenvironment. Most existing methods for tissue phenotyping are limited to the classification of tumor and stroma and require large amount of annotated histology images which are often not available. In the current work, we pose the problem of identifying distinct tissue phenotypes as finding communities in cellular graphs or networks. First, we train a deep neural network for cell detection and classification into five distinct cellular components. Considering the detected nuclei as nodes, potential cell-cell connections are assigned using Delaunay triangulation resulting in a cell-level graph. Based on this cell graph, a feature vector capturing potential cell-cell connection of different types of cells is computed. These feature vectors are used to construct a patch-level graph based on chi-square distance. We map patch-level nodes to the geometric space by representing each node as a vector of geodesic distances from other nodes in the network and iteratively drifting the patch nodes in the direction of positive density gradients towards maximum density regions. The proposed algorithm is evaluated on a publicly available dataset and another new large-scale dataset consisting of 280K patches of seven tissue phenotypes. The estimated communities have significant biological meanings as verified by the expert pathologists. A comparison with current state-of-the-art methods reveals significant performance improvement in tissue phenotyping.
KW - Cellular communities
KW - Computational pathology
KW - Tissue phenotyping
KW - Tumor microenvironment
UR - http://www.scopus.com/inward/record.url?scp=85083463418&partnerID=8YFLogxK
U2 - 10.1016/j.media.2020.101696
DO - 10.1016/j.media.2020.101696
M3 - Article
C2 - 32330851
AN - SCOPUS:85083463418
SN - 1361-8415
VL - 63
JO - Medical Image Analysis
JF - Medical Image Analysis
M1 - 101696
ER -